Canonical Allele Identifier: CA1844699076
Gene: TOPORS HGNC NCBI
SMIM27 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.32551158C= , CM000671.2:g.32551158C= GRCh38
NC_000009.11:g.32551156C= , CM000671.1:g.32551156C= GRCh37
NC_000009.10:g.32541156C= NCBI36
NG_017050.1:g.6467G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360538.7:c.4-190G= (TOPORS) MANE Select ENSP00000353735.2:n.4-190G=
ENST00000453396.5:n.15C= (SMIM27)
ENST00000680198.1:c.4-190G= ENSP00000505143.1:n.4-190G=
ENST00000681750.1:c.-239-190G= ENSP00000506413.1:n.-239-190G=
ENST00000360538.6:c.4-190G= (TOPORS) ENSP00000353735.2:n.4-190G=
ENST00000379858.1:c.3+1276G= (TOPORS) ENSP00000369187.1:n.3+1276G=
NM_001195622.1:c.3+1276G= (TOPORS) NP_001182551.1:n.3+1276G=
NM_005802.4:c.4-190G= (TOPORS) NP_005793.2:n.4-190G=
NR_033991.1:n.15C= (SMIM27)
NM_001349118.1:c.-737C= (SMIM27) NP_001336047.1:n.-737C=
XM_024447368.1:c.165C= (SMIM27) XP_024303136.1:p.Asp55=
NM_005802.5:c.4-190G= (TOPORS) MANE Select NP_005793.2:n.4-190G=
NM_001195622.2:c.3+1276G= (TOPORS) NP_001182551.1:n.3+1276G=